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Chemical Structure Cat. No. Product Name CAS No.
Sodium deoxycholate Chemical Structure
BCP46842 Sodium deoxycholate 302-95-4
Sodium deoxycholate is a bile acid salt. It contains a deoxycholate.
CY09 Chemical Structure
BCP29136 CY09 1073612-91-5
CY-09 is an NLRP3 inhibitor.
Sodium carboxymethyl cellulose Chemical Structure
BCP43883 Sodium carboxymethyl cellulose 9004-32-4
CMC can be used for a wide range of application such as:• food processing, textiles, detergents, and drugs• a stabilizer in the preparation of nanoparticles• a binder for the formation of electrodes
2-Methyl hexanal Chemical Structure
BCP49680 2-Methyl hexanal 925-54-2
Trans-Chalcone Chemical Structure
BCP14123 Trans-Chalcone 614-47-1
Chalcone is a member of the class of chalcones that is acetophenone in which one of the methyl hydrogens has been replaced by a benzylidene group. It has a role as a plant metabolite. It is a member of styrenes and a member of chalcones.
NNMTi Chemical Structure
BCP43790 NNMTi 42464-96-0
NNMTi is a nicotinamide N-methyltransferase (NNMT) inhibitor that promotes myoblast differentiation.
Conduritol B epoxide Chemical Structure
BCP07465 Conduritol B epoxide 6090-95-5
Conduritol B epoxide, also known as CBE, is an inhibitor of non-mammalian and mammalian β-glucosidase. When injected in mice it produces the biochemical and certain clinical and pathological characteristics of Gaucher disease. Conduritol B epoxide is a mechanism-based inhibitor which binds covalently to the catalytic site of acid β-glucosidase.
6-Ethyl-1,2,3,4-tetrahydroanthraquinone Chemical Structure
BCP06060 6-Ethyl-1,2,3,4-tetrahydroanthraquinone 15547-17-8
CYM-5478 Chemical Structure
BCP49679 CYM-5478 870762-83-7
CYM-5478 is a potent and highly selective S1P2 agonist with an EC50 of 119 nM in a TGFα-shedding assay. CYM-5478 protects neural-derived cell lines against Cisplatin toxicity.
D-Fructose 2,6-Diphosphate Sodium Salt Chemical Structure
BCP30518 D-Fructose 2,6-Diphosphate Sodium Salt 84364-89-6
D-Fructose 2,6-diphosphate sodium salt is a potent stimulator of 6-Phosphofructo-1-kinase (PFK-1) and also inhibits Fructose-1,6-Bisphosphatase.
DMCBDA Chemical Structure
BCP49590 DMCBDA 15894-21-0
Zinc trifluoromethanesulfonate Chemical Structure
BCP49678 Zinc trifluoromethanesulfonate 54010-75-2
Zinc trifluoromethanesulfonate is the zinc salt of trifluoromethanesulfonic acid.
Carfilzomib Chemical Structure
BCP02588 Carfilzomib 868540-17-4
Carfilzomib (PR-171) is an irreversible proteasome inhibitor with an IC50 of 5 nM in ANBL-6 and RPMI 8226 cells.
(Z)-Guggulsterone Chemical Structure
BCP07472 (Z)-Guggulsterone 39025-23-5
Z-guggulsterone, a constituent of Indian Ayurvedic medicinal plant Commiphora mukul, inhibits the growth of human prostate cancer cells by causing apoptosis. Z-guggulsterone inhibits angiogenesis by suppressing the VEGF–VEGF-R2–Akt signaling axis.
Teprenone Chemical Structure
BCP11723 Teprenone 6809-52-5
Teprenone can induce expression of HSP70, HSPB8, and HSPB1.
Sivelestat sodium tetrahydrate Chemical Structure
BCP09535 Sivelestat sodium tetrahydrate 201677-61-4
Sivelestat sodium tetrahydrate is a competitive inhibitor of human neutrophil elastase, also inhibits leukocyte elastase obtained from rabbit, rat, hamster and mouse.
Verteporfin Chemical Structure
BCP04238 Verteporfin 129497-78-5
Verteporfin, a benzoporphyrin derivative, is a medication used as a photosensitizer for photodynamic therapy.
5-Fluorouridine Chemical Structure
BCP20793 5-Fluorouridine 77180-80-4
5-Fluorouridine showcases its antiviral properties. This concoction exerts a inhibitory efficacy against certain RNA virus strains.
Amino-PEG2-Amine Chemical Structure
BCP43929 Amino-PEG2-Amine 929-59-9
Amino-PEG2-Amine(PROTAC Linker 19) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.
Decapeptide-4 Chemical Structure
BCP49672 Decapeptide-4 Decapeptide-4
Decapeptide-4 is a synthetic peptide consisting of arginine, aspartic acid, cysteine, glutamic acid, leucine, methionine and tyrosine.
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